Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 17 |
NetGPI | no | yes: 0, no: 17 |
Related structures:
AlphaFold database: Q4QB18
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 483 | 487 | PF00656 | 0.430 |
CLV_MEL_PAP_1 | 478 | 484 | PF00089 | 0.283 |
CLV_NRD_NRD_1 | 172 | 174 | PF00675 | 0.744 |
CLV_NRD_NRD_1 | 498 | 500 | PF00675 | 0.316 |
CLV_NRD_NRD_1 | 624 | 626 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 645 | 647 | PF00675 | 0.429 |
CLV_PCSK_KEX2_1 | 141 | 143 | PF00082 | 0.630 |
CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.692 |
CLV_PCSK_KEX2_1 | 337 | 339 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 498 | 500 | PF00082 | 0.316 |
CLV_PCSK_KEX2_1 | 624 | 626 | PF00082 | 0.481 |
CLV_PCSK_KEX2_1 | 645 | 647 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 672 | 674 | PF00082 | 0.508 |
CLV_PCSK_PC1ET2_1 | 141 | 143 | PF00082 | 0.552 |
CLV_PCSK_PC1ET2_1 | 337 | 339 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 645 | 647 | PF00082 | 0.412 |
CLV_PCSK_PC1ET2_1 | 672 | 674 | PF00082 | 0.508 |
CLV_PCSK_PC7_1 | 620 | 626 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 141 | 145 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 308 | 312 | PF00082 | 0.394 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.449 |
CLV_PCSK_SKI1_1 | 433 | 437 | PF00082 | 0.310 |
CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.718 |
CLV_PCSK_SKI1_1 | 612 | 616 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 620 | 624 | PF00082 | 0.368 |
DEG_SCF_FBW7_2 | 418 | 423 | PF00400 | 0.417 |
DEG_SPOP_SBC_1 | 183 | 187 | PF00917 | 0.511 |
DOC_CYCLIN_yCln2_LP_2 | 552 | 558 | PF00134 | 0.422 |
DOC_MAPK_gen_1 | 191 | 201 | PF00069 | 0.460 |
DOC_MAPK_gen_1 | 243 | 250 | PF00069 | 0.306 |
DOC_MAPK_HePTP_8 | 435 | 447 | PF00069 | 0.276 |
DOC_MAPK_MEF2A_6 | 438 | 447 | PF00069 | 0.277 |
DOC_PP1_RVXF_1 | 126 | 133 | PF00149 | 0.501 |
DOC_PP1_RVXF_1 | 479 | 485 | PF00149 | 0.306 |
DOC_PP2B_LxvP_1 | 367 | 370 | PF13499 | 0.519 |
DOC_PP4_FxxP_1 | 665 | 668 | PF00568 | 0.389 |
DOC_USP7_MATH_1 | 151 | 155 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 165 | 169 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 182 | 186 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 195 | 199 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 480 | 484 | PF00917 | 0.283 |
DOC_USP7_MATH_1 | 600 | 604 | PF00917 | 0.379 |
DOC_USP7_MATH_1 | 9 | 13 | PF00917 | 0.687 |
DOC_USP7_UBL2_3 | 641 | 645 | PF12436 | 0.390 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 286 | 291 | PF00397 | 0.396 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 509 | 514 | PF00397 | 0.458 |
DOC_WW_Pin1_4 | 54 | 59 | PF00397 | 0.667 |
LIG_14-3-3_CanoR_1 | 110 | 119 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 142 | 150 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 24 | 29 | PF00244 | 0.464 |
LIG_14-3-3_CanoR_1 | 481 | 485 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 624 | 632 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 679 | 683 | PF00244 | 0.615 |
LIG_BRCT_BRCA1_1 | 11 | 15 | PF00533 | 0.486 |
LIG_BRCT_BRCA1_1 | 288 | 292 | PF00533 | 0.382 |
LIG_BRCT_BRCA1_1 | 504 | 508 | PF00533 | 0.325 |
LIG_CSL_BTD_1 | 205 | 208 | PF09270 | 0.357 |
LIG_CSL_BTD_1 | 296 | 299 | PF09270 | 0.303 |
LIG_EH1_1 | 636 | 644 | PF00400 | 0.509 |
LIG_EVH1_2 | 119 | 123 | PF00568 | 0.361 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.296 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.654 |
LIG_FHA_1 | 23 | 29 | PF00498 | 0.438 |
LIG_FHA_1 | 279 | 285 | PF00498 | 0.450 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.432 |
LIG_FHA_1 | 417 | 423 | PF00498 | 0.400 |
LIG_FHA_1 | 560 | 566 | PF00498 | 0.416 |
LIG_FHA_1 | 638 | 644 | PF00498 | 0.430 |
LIG_FHA_1 | 646 | 652 | PF00498 | 0.447 |
LIG_FHA_2 | 16 | 22 | PF00498 | 0.638 |
LIG_FHA_2 | 345 | 351 | PF00498 | 0.525 |
LIG_FHA_2 | 510 | 516 | PF00498 | 0.446 |
LIG_FHA_2 | 569 | 575 | PF00498 | 0.358 |
LIG_FHA_2 | 673 | 679 | PF00498 | 0.541 |
LIG_LIR_Apic_2 | 253 | 257 | PF02991 | 0.352 |
LIG_LIR_Apic_2 | 258 | 263 | PF02991 | 0.388 |
LIG_LIR_Apic_2 | 384 | 388 | PF02991 | 0.408 |
LIG_LIR_Apic_2 | 664 | 668 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 121 | 131 | PF02991 | 0.284 |
LIG_LIR_Gen_1 | 144 | 153 | PF02991 | 0.473 |
LIG_LIR_Gen_1 | 202 | 212 | PF02991 | 0.339 |
LIG_LIR_Gen_1 | 246 | 254 | PF02991 | 0.321 |
LIG_LIR_Gen_1 | 32 | 41 | PF02991 | 0.383 |
LIG_LIR_Gen_1 | 459 | 467 | PF02991 | 0.457 |
LIG_LIR_LC3C_4 | 640 | 644 | PF02991 | 0.517 |
LIG_LIR_Nem_3 | 121 | 126 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 202 | 207 | PF02991 | 0.353 |
LIG_LIR_Nem_3 | 246 | 250 | PF02991 | 0.318 |
LIG_LIR_Nem_3 | 430 | 435 | PF02991 | 0.275 |
LIG_LIR_Nem_3 | 621 | 626 | PF02991 | 0.375 |
LIG_NRBOX | 15 | 21 | PF00104 | 0.409 |
LIG_NRP_CendR_1 | 690 | 693 | PF00754 | 0.630 |
LIG_PALB2_WD40_1 | 118 | 126 | PF16756 | 0.364 |
LIG_PCNA_PIPBox_1 | 93 | 102 | PF02747 | 0.418 |
LIG_Pex14_2 | 256 | 260 | PF04695 | 0.468 |
LIG_Pex14_2 | 432 | 436 | PF04695 | 0.294 |
LIG_Pex14_2 | 461 | 465 | PF04695 | 0.359 |
LIG_Pex14_2 | 500 | 504 | PF04695 | 0.338 |
LIG_PTB_Apo_2 | 564 | 571 | PF02174 | 0.371 |
LIG_PTB_Phospho_1 | 564 | 570 | PF10480 | 0.371 |
LIG_SH2_NCK_1 | 385 | 389 | PF00017 | 0.409 |
LIG_SH2_PTP2 | 204 | 207 | PF00017 | 0.456 |
LIG_SH2_SRC | 366 | 369 | PF00017 | 0.516 |
LIG_SH2_SRC | 385 | 388 | PF00017 | 0.253 |
LIG_SH2_SRC | 47 | 50 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 663 | 667 | PF00017 | 0.390 |
LIG_SH2_STAT3 | 374 | 377 | PF00017 | 0.492 |
LIG_SH2_STAT3 | 522 | 525 | PF00017 | 0.313 |
LIG_SH2_STAT3 | 570 | 573 | PF00017 | 0.429 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 247 | 250 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.523 |
LIG_SH2_STAT5 | 522 | 525 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 570 | 573 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 582 | 585 | PF00017 | 0.386 |
LIG_SH3_1 | 452 | 458 | PF00018 | 0.347 |
LIG_SH3_2 | 83 | 88 | PF14604 | 0.432 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.584 |
LIG_SH3_3 | 202 | 208 | PF00018 | 0.472 |
LIG_SH3_3 | 274 | 280 | PF00018 | 0.488 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.397 |
LIG_SH3_3 | 296 | 302 | PF00018 | 0.419 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.472 |
LIG_SH3_3 | 448 | 454 | PF00018 | 0.322 |
LIG_SH3_3 | 479 | 485 | PF00018 | 0.323 |
LIG_SH3_3 | 80 | 86 | PF00018 | 0.504 |
LIG_SUMO_SIM_par_1 | 210 | 216 | PF11976 | 0.442 |
LIG_SUMO_SIM_par_1 | 24 | 32 | PF11976 | 0.499 |
LIG_TRAF2_1 | 158 | 161 | PF00917 | 0.419 |
LIG_TRAF2_1 | 347 | 350 | PF00917 | 0.554 |
LIG_TRAF2_1 | 571 | 574 | PF00917 | 0.414 |
LIG_TRFH_1 | 395 | 399 | PF08558 | 0.447 |
LIG_UBA3_1 | 431 | 438 | PF00899 | 0.295 |
LIG_WRC_WIRS_1 | 311 | 316 | PF05994 | 0.464 |
LIG_WW_2 | 179 | 182 | PF00397 | 0.506 |
MOD_CDK_SPK_2 | 54 | 59 | PF00069 | 0.518 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.549 |
MOD_CK1_1 | 168 | 174 | PF00069 | 0.566 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.688 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.368 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.351 |
MOD_CK2_1 | 15 | 21 | PF00069 | 0.468 |
MOD_CK2_1 | 344 | 350 | PF00069 | 0.494 |
MOD_CK2_1 | 568 | 574 | PF00069 | 0.363 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.566 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.452 |
MOD_GlcNHglycan | 167 | 170 | PF01048 | 0.691 |
MOD_GlcNHglycan | 186 | 189 | PF01048 | 0.652 |
MOD_GlcNHglycan | 447 | 450 | PF01048 | 0.344 |
MOD_GlcNHglycan | 602 | 605 | PF01048 | 0.336 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.665 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.577 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.729 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.347 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.524 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.380 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.434 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.366 |
MOD_GSK3_1 | 668 | 675 | PF00069 | 0.488 |
MOD_LATS_1 | 406 | 412 | PF00433 | 0.455 |
MOD_N-GLC_2 | 489 | 491 | PF02516 | 0.342 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.641 |
MOD_NEK2_1 | 15 | 20 | PF00069 | 0.447 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.375 |
MOD_NEK2_1 | 28 | 33 | PF00069 | 0.565 |
MOD_NEK2_1 | 402 | 407 | PF00069 | 0.358 |
MOD_NEK2_2 | 516 | 521 | PF00069 | 0.426 |
MOD_PIKK_1 | 265 | 271 | PF00454 | 0.442 |
MOD_PIKK_1 | 345 | 351 | PF00454 | 0.577 |
MOD_PIKK_1 | 465 | 471 | PF00454 | 0.387 |
MOD_PKA_1 | 141 | 147 | PF00069 | 0.496 |
MOD_PKA_1 | 645 | 651 | PF00069 | 0.383 |
MOD_PKA_1 | 672 | 678 | PF00069 | 0.537 |
MOD_PKA_2 | 141 | 147 | PF00069 | 0.466 |
MOD_PKA_2 | 480 | 486 | PF00069 | 0.395 |
MOD_PKA_2 | 645 | 651 | PF00069 | 0.383 |
MOD_PKA_2 | 672 | 678 | PF00069 | 0.537 |
MOD_Plk_1 | 195 | 201 | PF00069 | 0.510 |
MOD_Plk_2-3 | 678 | 684 | PF00069 | 0.485 |
MOD_Plk_4 | 11 | 17 | PF00069 | 0.481 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.417 |
MOD_Plk_4 | 427 | 433 | PF00069 | 0.319 |
MOD_Plk_4 | 516 | 522 | PF00069 | 0.417 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.407 |
MOD_ProDKin_1 | 286 | 292 | PF00069 | 0.392 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.469 |
MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.440 |
MOD_ProDKin_1 | 509 | 515 | PF00069 | 0.453 |
MOD_ProDKin_1 | 54 | 60 | PF00069 | 0.675 |
MOD_SUMO_rev_2 | 444 | 454 | PF00179 | 0.324 |
MOD_SUMO_rev_2 | 70 | 76 | PF00179 | 0.698 |
TRG_DiLeu_BaEn_2 | 458 | 464 | PF01217 | 0.382 |
TRG_DiLeu_BaLyEn_6 | 269 | 274 | PF01217 | 0.444 |
TRG_DiLeu_BaLyEn_6 | 387 | 392 | PF01217 | 0.370 |
TRG_DiLeu_BaLyEn_6 | 654 | 659 | PF01217 | 0.410 |
TRG_DiLeu_BaLyEn_6 | 687 | 692 | PF01217 | 0.590 |
TRG_ENDOCYTIC_2 | 204 | 207 | PF00928 | 0.382 |
TRG_ENDOCYTIC_2 | 247 | 250 | PF00928 | 0.327 |
TRG_ENDOCYTIC_2 | 333 | 336 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 35 | 38 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 521 | 524 | PF00928 | 0.477 |
TRG_ER_diArg_1 | 498 | 500 | PF00400 | 0.319 |
TRG_ER_diArg_1 | 539 | 542 | PF00400 | 0.365 |
TRG_ER_diArg_1 | 623 | 625 | PF00400 | 0.477 |
TRG_NES_CRM1_1 | 442 | 457 | PF08389 | 0.335 |
TRG_NLS_MonoExtC_3 | 644 | 649 | PF00514 | 0.404 |
TRG_Pf-PMV_PEXEL_1 | 110 | 114 | PF00026 | 0.531 |
TRG_Pf-PMV_PEXEL_1 | 272 | 276 | PF00026 | 0.457 |
TRG_Pf-PMV_PEXEL_1 | 649 | 653 | PF00026 | 0.365 |
TRG_Pf-PMV_PEXEL_1 | 657 | 661 | PF00026 | 0.413 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBN6 | Leptomonas seymouri | 76% | 99% |
A0A0S4ISW7 | Bodo saltans | 49% | 93% |
A0A1X0NY35 | Trypanosomatidae | 59% | 99% |
A0A3Q8IBV8 | Leishmania donovani | 96% | 82% |
A0A3Q8IE69 | Leishmania donovani | 27% | 100% |
A0A3R7MZ34 | Trypanosoma rangeli | 60% | 100% |
A4HAI4 | Leishmania braziliensis | 26% | 100% |
A4HD07 | Leishmania braziliensis | 90% | 89% |
A4I0J3 | Leishmania infantum | 96% | 82% |
C9ZN08 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
C9ZVC0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
E9AHS5 | Leishmania infantum | 27% | 100% |
E9AWF4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
E9B4P5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
Q4Q3D1 | Leishmania major | 27% | 100% |
V5BEM5 | Trypanosoma cruzi | 54% | 100% |